Highly Transparent and Flexible Triboelectric Nanogenerators with

Subscriber access provided by Stockholm University Library

Article

Highly-transparent and flexible triboelectric nanogenerators with subwavelength architectured PDMS by nanoporous anodic aluminum oxide template Bhaskar Dudem, Yeong Hwan Ko, Jung Woo Leem, Soo Hyun Lee, and Jae Su Yu ACS Appl. Mater. Interfaces, Just Accepted Manuscript • DOI: 10.1021/acsami.5b05842 • Publication Date (Web): 24 Aug 2015 Downloaded from http://pubs.acs.org on August 25, 2015

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

ACS Applied Materials & Interfaces is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Materials & Interfaces

Highly-transparent and flexible triboelectric nanogenerators with subwavelength

architectured

PDMS

by

nanoporous

anodic

aluminum oxide template Bhaskar Dudem, Yeong Hwan Ko, Jung Woo Leem, Soo Hyun Lee, and Jae Su Yu∗ Department of Electronics and Radio Engineering, Kyung Hee University, 1732 Deogyeongdaero, Giheung-gu,Yongin-si, 446-701, South Korea

ABSTRACT Highly-transparent and flexible triboelectric nanogenerators (TENGs) were fabricated using the subwavelength architectured (SWA) polydimethysiloxane (PDMS) by nanoporous anodic aluminum oxide (AAO) template as a replica mold. The SWA PDMS could be utilized as a multi-functional film for the triboelectric layer, antireflection coating, and self-cleaning surface. The nanopore arrays of AAO were formed by a simple, fast, and cost-effective electrochemical oxidation process of aluminum, which is relatively impressive to fabricate the TENG device. For electrical contacts, the SWA PDMS was laminated on the indium tin oxide (ITO)-coated polyethylene terephthalate (PET) as a bottom electrode and the bare ITO-coated PET (i.e., ITO/PET) was used for a top electrode. Compared to the ITO/PET, the SWA PDMS on the ITO/PET improved the transmittance from 80.5 to 83% in the visible wavelength region and also had high transmittances of > 85% at wavelengths of 430-455 nm. The SWA PDMS also exhibited the hydrophobic surface with a critical angle (θCA) value of ∼115o, which can be useful for self-cleaning applications. The average transmittance (Tavg) of entire TENG device was observed to be about 70% over a broad wavlength range. At the external pushing frequency of

∗

Author to whom correspondence should be addressed. Electronic mail: [email protected] 1

ACS Paragon Plus Environment


1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 2 of 30

0.5 Hz, the TENG device with the ITO top electrode, the open-circuit voltage (VOC) and shortcircuit current (ISC) values of ∼ 3.8 V and ∼ 0.8 µA were generated instantaneously, respectively, which were higher than those (i.e., VOC ≈ 2.2 V and ISC ≈ 0.4 µA) of the TENG device with a gold top electrode. The effect of external pushing force and frequency on the output device performance of the TENGs was investigated, including the device robustness. The theoretical optical analysis of SWA PDMS was also performed.

KEYWORDS: Transperency, triboelectric nanogenerators, subwavelength architectured PDMS, anodic aluminum oxide

INTRODUCTION Energy conversion technology from ambient environment sources into electrical energy is one of great interest in various renewable energy applications and it has been expected for the foremost substitution for conventional power supplies.1-3 Currently, nanogenerators have exhibited the promising potential to efficiently convert different forms of energies into electricity using piezoelectrics, trioelectrics, electromagnetics, and pyroelectric effects.4-7 Especially, most of the researchers in the field have a growing interest on triboelectric nanogenerators (TENGs) because of their conversion efficiency of various mechanical energies observed in our daily lifes such as human motion,8,9 mechanical triggering, 10-12 rotation,13,14 etc. According to general operation principle of TENGs, the electron flow can take place by the triboelectric effect induced electrostatic charges on the surfaces of two different triboelectric materials.15 However, there are still technological demands for the next generation of flexible and transparent device applications. Triboelectric nanogenerators can be also utilized for various applications such as self-powered sensors to recognize the human motion/pressure, voice recognition, transportation monitoring, 2


Page 3 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


and so on.16-21 Many research groups demonstrated flexible and transparent piezoelectric zinc oxide (ZnO)-based nanogenerators, but the design process of devices is somewhat complex in connection with sophisticated operations.22,23 Recently, flexible TENGs based on polymer materials have been developed rapidly due to their simple and cost-effective design process with high output performance as compared to other nanogenerators as a power sources.24-28 These flexible TENGs have been demonstrated by employing the micro- and nano-patterned polymer materials such as polydimethylsiloxane (PDMS) as a triboelectric material, where the indium tin oxide (ITO)-coated polyethylene terephthalate (PET) or gold (Au) is used as an electrode. In general, the patterned PDMS surface plays a key role in increasing the separation efficiency and the friction area between the polymer materials and electrodes, thereby improving the device efficiency.27,29,30 Simultaneously, these patterned structures on the PDMS can also improve the transparency of the TENGs with a transparent conductive oxide-coated film like the ITO owing to the antireflection property of patterned PDMS.27 To prepare the micro- or nano-patterns on the surface of PDMS using softlithography, silicon (Si) or sapphire molds have been generally employed. However, the fabrication of these patterned surfaces involves expensive processing techniques such as photolithography,29 electron-beam lithography,31 nano imprinting lithography,32 laser interference lithography,33,34 etc., including a subsequent dry etching. Moreover, the fabrication process of these molds is complicated and consumes a long time. On the other hand, a nanoporous anodic aluminum oxide (AAO) template is one of the best alternatives to these molds. The AAO templates have been prepared by a simple, fast, and cost-effective electrochemical oxidation process (anodization) of aluminum (Al) under certain electrolyte conditions. The AAO is an aluminium oxide (Al2O3) film with self-organized and closely-packed cylindrical nanopores.35,36 3



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 4 of 30

In this work, we reported the triboelectric characteristics of highly-transparent and flexible PDMS layer with subwavelength architectures (i.e., SWA PDMS) fabricated by a softlithography technique via the porous AAO template as a mold. The SWA PDMS significantly improves the transparent property of TENG devices in the broad visible and near-infrared wavelength range of 400-1000 nm as well as the efficient friction surface compared to the bare flat PDMS. Besides, it can be easily prepared by the mass-productive soft lithography method which consumes the low cost and short time with large scalability since once AAO molds are fabricated, they can be repeatedly used for pattern formations on the PDMS surface. In addition, due to the detachability of the PDMS on any flat transparent substrates, the damaged SWA PDMS can be just replaced into new one in TENG device systems. Also, the SWA PDMS with a hydrophobic surface can be utilized in self-cleaning applications. In this point, we proposed the highly-roughened SWA PDMS which offers an efficient surface for triboelectric charge generations as well as a high transparency. Optical properties of the SWA PDMS layer on ITO/PET were measured and also studied therotically using a rigorous coupled-wave analysis (RCWA) simulation. The SWA PDMS layer was laminated on the ITO/PET to fabticate higlytransparent and flexible TENG devices and their output voltage and current performance were explored.

EXPERIMENTAL DETAILS Figure 1 shows the schematic for the fabrication of the TENG device with the SWA PDMS layer laminated on the ITO/PET substrate as a bottom electrode and the bare ITO/PET as a top electrode. To prepare the SWA PDMS, the nanoporous AAO template on Si (i.e., AAO/Si) as a replica mold was used. The AAO template was fabricated by the anodization of Al thin film with

4


Page 5 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


200 nm of thickness which was deposited on the Si substrate by using an electron-beam evaporation system at room temperature. The Al thin film was further anodized using 5 wt% H3PO4 electrolyte solution at applied DC voltage of 75 V and the pore widening treatment was carried out by dipping the anodized samples for 10 min into 5 wt% phosphoric acid solution at 30 °C, which forms AAO nanopore arrays. During the anodization process, the temperature of the electrolyte was maintained at 2 °C. Then, the surface of the anodized sample (i.e., AAO template) was treated with tri-methylchlorosilane gas phase silanization for 4 hr to prevent the PDMS film from sticking to the porous AAO. Furthermore, the random nanopatterns on template were transferred by spin-coating the hard PDMS (h-PDMS, prepared by mixing the VDT-731, SIP 6831.1, SIT 7900, and HMS-301 from Gelest, Inc.) on the surface of AAO/Si substrate and then cured in oven at 75 °C for 20 min. Subsequently, the soft PDMS (s-PDMS: mixture of base resin and curing agent of Sylgard 184 silicone elastomer) was also spin-coated on the hPDMS/AAO/Si substrate and cured again at 80 °C for 2 hr. Here, we spin-coated two different PDMS (h- and s-PDMS) layers on the AAO/Si mold at different spin-coating conditions (as mentioned in the Supporting Information). As compared to the s-PDMS with low modulus ∼2 N/mm2, the h-PDMS with high modulus (∼9 N/mm2) and low surface energy could be useful to replicate high-density nanoporous structures on the AAO at the 100-nm scale without any distortion and deformation.37,38 But it is difficult to handle a thin (∼30µm) and stiff layer of hPDMS.39 Therefore, the s-PDMS was spin coated on the stiff h-PDMS as a protecting layer and enables for manual application, in a non-destructive manner.40,41 Finally, a thermally cured PDMS (h-/s-PDMS) layer containing the subwavelength architectures (SWAs) on the surface was peeled off from the AAO/Si substrate. Subsequently, the SWA PDMS layer was carefully laminated on the insulation surface of a clean ITO-coated PET substrate, and then the entire 5



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 6 of 30

structure was covered with another ITO-coated PET film (or Au-coated ITO/PET film) to form the sandwich-structured TENG devices, as shown in Figure 1. It is noted that the SWA PDMS surface and the ITO electrode (or Au electrode) are placed face to face, and separated by leaving a 3 mm gap between two contact surfaces using glass spacers. The device fabrication process is very simple and low-cost, and it can be useful for large-scale production industries. For comparison, the bare PDMS with the flat surface was also prepared by the same process, and then it was also applied into TENG devices. The structural and morphological properties of the AAO template fabricated on Si substrates and the SWA PDMS replicated by AAO templates were observed by using a field-emission scanning electron microscope (FE-SEM; LEO SUPRA 55, Carl Zeiss) measurements. The transmittance nature of samples was evaluated by using a UV-vis-NIR spectrophotometer (Cary 5000, Varian) with an integrating sphere at normal incidence. The water contact angles were measured and averaged at three different positions on the surface of samples by using a contact angle measurement system (Phoenix-300, SEO Co., Ltd.) with ∼5 µL droplets of deionized water at room temperature. For theoretical analysis of the SWA PDMS on the ITO/PET substrate, optical modeling and simulation were performed by the RCWA method using a commercial software (DiffractMOD, Rsoft Design Group). To design the theoretical models, the PDMS layer with subwavelength architectures was roughly considered as cylindrical pattern arrays with a periodic four-fold rectangular symmetry, for simplicity. The generated open-circuit voltage (VOC) and short-circuit current (ISC) of the fabricated TENG device were measured by using a programmable Keithley 2000 system as a multimeter and a Keithley 6487 system as a picoammeter, respectively. An indicator with a load cell (BONGSHIN, Inc.) was used to monitor the external pushing force applied on the top electrode of TENG devices.

6


Page 7 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


RESULTS AND DISCUSSIONS To investigate the influence of SWA PDMS laminated on ITO/PET on the total transmittance, the RCWA simulation was performed. Figure 2a shows the contour plot of the calculated transmittance spectra by considering a simple three-dimensional (3D) scale-modified simulation model with periodic four-fold rectangular symmetry SWA arrays (also shown in Figure 2a). We assumed that the each thickness of PDMS, PET, and ITO was fixed to be 100 µm, 130 µm, and 200 nm, respectively. The period and height of SWAs were set to be 155 nm and 180 nm, respectively, as observed by FE-SEM images (see Figure 3a). In Figure 2a, as the diameter to period ratio (RDP) of SWAs on PDMS is increased up to 0.65, the total transmittance over a wavelength range of 400-460 nm is also increased, and then it is gradually decreased at larger RDP values of 0.65. It is also found that, at the RDP value of 0.65 for SWAs with a 100 nm the diameter, the total transmittance is higher than 85% over a wavelength range of 400-460 nm. Moreover, at RDP values of 0.6-0.7, the high average transmittance can be observed over a long wavelength region of 580-800 nm. From theoretical simulations, it is possible to achieve high transmittance in the PDMS layer when the diameter of SWAs is about 100 nm. To achieve the transparent TENG device, a highly-transparent SWA PDMS film and two transparent ITO-coated PET films as the top and bottom electrodes, respectively, were used to construct the entire device (Device-I). At the same time, we also fabricated another device (Device-II) by replacing the bare ITO/PET as a top electrode with the Au-coated ITO/PET. From the previous reports, it is very clear that polymer-electrode based TENGs have a stronger ability to exchange triboelectric charges compared to polymer-polymer based TENGs.42 To design the polymer-electrode based TENG device, the two different electrodes (ITO and Au) were employed and the output

7



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 8 of 30

performance and transmittance of both devices were compared. The measured transmittance spectra of the TENG devices and their constituent materials in the wavelength range of 380-1000 nm are shown in Figure 2b. The flat PDMS laminated on the PET surface of ITO/PET substrate exhibited a improved average transmittance (Tavg ≈ 82%) compared to the bare ITO/PET substrate (Tavg ≈ 80.5%) in the visible and near infrared wavelength region. This increase in the transmittance spectra is due to the step gradient refractive index profile of air (n = 1)/PDMS (n ≈ 1.4)/PET (n ≈ 1.6). However, for the SWA PDMS laminated on ITO/PET substrate, the average transmittance (Tavg ≈ 83%) was further enhanced and its total transmittance was higher than 85% over a wavelength range of 430-455 nm. From this, the SWAs can more effectively reduce the surface reflection due to a continuous linear gradient in effective refractive index between air and the PDMS.29,37 For the entire TENG device (Device-I), the high Tavg value of ~ 70% was achieved at wavlengths of 400-1000 nm. Another TENG device (Device-II) exhibited a significantly lower average transmittance of ∼ 0.4% as compared with the Device-I, this is attributed to the replacement of the Au-coated ITO/PET (Tavg ≈ 0.5%) with the bare ITO/PET (Tavg ≈ 81%) as a top electrode. Figure 3a shows the top-view and cross-sectional SEM images of the nanoporous AAO template on Si substrate. The SEM images of the SWA PDMS (using h-/s-PDMS) layer replicated by the AAO template are also shown. To examine the feasibility of nanostructures imprint by AAO template, the h-PDMS and s- PDMS layers were compared each other, as shown in Figure S1 (See the Supporting Information). The corresponding SEM images in Figure S1 reveal that the only s-PDMS is not suitable to replicate the AAO nanofeatures on the surface of PDMS layer due to its lower modulus of ~ 2 N/mm2 than that (i.e., ~ 9 N/mm2) of h-PDMS. The SEM images in (i) and (iii) of Figure 3a reveal that the average pore diameter, period, and height

8


Page 9 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


of AAO nanopores were approximately 100 nm, 160 nm, and 210 nm, respectively. The SEM images in (ii) and (iv) of Figure 3a show the uniformly distributed SWA arrays on the surface of PDMS, with average diameter and height of about 100 nm and 180 nm, respectively. The diameter and height of the SWAs were similar to the pore diameter and height of nanoporous AAO template. Most of the SWAs were vertically-oriented on the substrate, which produces shapes like a bunch due to the attraction forces among the SWAs of PDMS when they were pulled out from the AAO template. Total thickness of the replicated PDMS layer was observed to be about 100 µm, as can be seen in the inset (iv) of Figure 3a. In Figure 3b, the photograph clarified that the SWA PDMS on ITO/PET is more transparent under the florescent light as compared to the flat PDMS on ITO/PET. To explore the surface wettability of the flat and SWA PDMS, the water contact angle was estimated, both the samples (see Figure 3b) showed a hydrophobic surface with water contact angles (θCA) > 90°. However, the SWA PDMS exhibited the larger θCA value of ~ 115° than that (i.e., θCA ~ 93°) of the flat PDMS.41,43 This SWA PDMS film with a hydrophobic surface (i.e., θCA ≈ 115°) can be utilized for self-cleaning applications.41 The working principle of the TENG device to generate the electrical energy was explained in Figure 4a. At original position (i), two electrodes are separated with a constant distance (~ 3 mm) under the absence of external pushing force. When an external pushing force is applied to the top electrode of TENG device (ii), the ITO film of ITO/PET substrate and the SWA PDMS film come into contact. As a result, owing to the different triboelectric coefficients of SWA PDMS and ITO materials, the opposite electrostatic charges are induced on each electrode. The positive triboelectric charges are accumulated on the ITO and the negative charges are induced on the PDMS side.30,44 By releasing the applied pushing force from the device (iii), two electrodes move apart from each other and produce the induced potential difference across the electrodes.

9



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 10 of 30

This potential difference leads to drive the electrons from the bottom electrode to the top electrode, and thus forms the negative current. When the device electrodes revert back to their original positions (iv), the triboelectric charge distribution reaches electrical equilibrium. Subsequently, as the external pushing force is applied once again (v), the electrons are driven towards the bottom electrode due to the reversed induced potential difference across the electrodes, which results in the positive current. To evaluate the performance of the TENG devices, a pressure indicator with a load cell (BONGSHIN, Inc.) was used to monitor (or adjust) the external pushing force to the device, with controlled frequencies using a metronome,22,23 as shown in Figure S2 (See the Supporting Information). The VOC curves generated by two different types of TENG devices (Device-I and Device-II) under 0.5 Hz of external pushing frequency and 0.3 kgf of external pushing force are shown in Figure 4b. The averaged VOC values of the Device-I and Device-II were observed as ∼ 3.8 and ∼ 2.2 V, respectively, in the shortest time interval (∼ 0.25 sec). These VOC values are relatively low compared to those (i.e., VOC > 10-200 V) reported on the PDMS-based TENG devices in previous works.42,45,46 In general, however, the output voltage is directly not only proportional to the triboelectric surface charge density (σ), but also relates to the capacitance of the device.47-50 Moreover, the σ is mainly affected by the intrinsic material properties of triboelectric (dielectric material) layer, the size of the dielectric and the gap between the top electrode and dielectric as well as the roughness of the contact surfaces. Thus, it is necessary to improve the output voltage of TENG devices by further optimizing the area of SWA PDMS or the gap between SWA PDMS and top electrode. To optimize the space distance between the SWA PDMS and the top electrode of TENG device, we tested the influence of spacer thickness of TENG device on the device output performance, as shown in Figure S3 (See the Supporting Information). From these results, we obtained the 10


Page 11 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


optimum spacer thickness of 3 mm for the TENG device, exhibiting stable and continuous output device performance, As a result, we used it in this experiment. Under the same condition, the ISC curves of these devices were measured, as shown in Figure 4c. At pressing and releasing moments on the device, the current peak directions were followed as indicated in Figure 4c and they were well consistent with the charge flow of the schematic diagram in Figure 4a. The Device-I and Device-II exhibited the averaged ISC values of about 0.8 and 0.4 µA, respectively, in the short time interval (∼ 0.16 and 0.14 sec, respectively). From the above results, the output performance of the Device-I is higher than that of the Device-II. This may be the reason that the ITO (top electrode of Device-I) has a better friction surface to easily contact with the PDMS surface, and thus it can sufficiently transfer more electrons into the device compared to the Aucoated ITO (top electrode of Device-II) surface, resulting in the superior output device performance. It is also noticeable that the transmittance of the Device-I is very high than that of the Device-II. Due to the high transmittance and output performance, the Device-I with ITO/PET as a top electrode was further studied, with maintaining a transparent property. Moreover, to study the influence of the patterned PDMS surface (SWA PDMS) on the device performance, we measured the TENG output performance using the flat PDMS as a triboelectric material instead of SWA PDMS as shown in the Figure 4d. The results clearly show that the output performance of TENG (VOC and ISC values of ∼ 1.5 V and 0.13 µA, respectively) was relatively lower than that of TENG using the SWA PDMS. The increased surface area by SWA PDMS can be expected to offer enhanced triboelectric charges due to the large friction area, while the insufficient friction area between the flat PDMS and electrodes does not properly produce the triboelectric charges.51,52 Figure 5a shows the photographic images of the fabricated transparent TENG device by

11



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 12 of 30

highlighting the features of (i) transparency and (ii) flexibility. This image supports the high transmittance from measured transmittance data (see Figure 2b) and the device can be viewed by the colored background. The photographic images for the pushing test with a highly-transparent and flexible TENG device are also shown in (iii) of Figure 5a. By using a load cell, a pushing force applied externally to the top electrode generates the electrostatic charges on the electrode surfaces according to the triboelectric tendency, as explained in Figure 4(a). To examine the influence of external pushing frequency on the output performance of the transparent TENG device, the (i) VOC and (ii) ISC curves were measured at different external pushing frequencies from 1 to 4 Hz as shown in Figure 5b. During these measurements, the external pushing force was maintained constantly at 0.3 kgf. It is evident that the VOC and ISC were gradually increased with increasing the external pushing frequency. As the external pushing frequency increased from 1 to 4 Hz, the averaged voltage/current values were increased from ∼ 4.8 V/ 1.2 µA to ∼ 11.6 V/ 2.11 µA, respectively. As the external pushing frequency was increased, the output performance of the TENG was improved by the highly accumulated residual charges on the surfaces of both electrodes due to the faster pushing cycle, thus leading to the increase of triboelectric potential.51 Figure 5c shows the measured (i) VOC and (ii) ISC curves of the transparent TENG device under 1 Hz of external pushing frequency at different external pushing forces. As can be seen in the measured output curves, it can be known that the electric output of TENG device is strongly related to the external pushing force and so the highest output can be observed under the largest external applied force. At a small pushing force range of 0.3-0.5 kgf, the averaged VOC and ISC values of the TENG device were obtained to be ∼ 5.1 V and ∼ 1.22 µA, respectively. When the external pushing force increased to 1.7-1.9 kgf, the averaged VOC and ISC values were increased to ∼ 10.2 V and ∼ 1.68 µA. This result is caused by the increased contact

12


Page 13 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


area and the deformation of PDMS under the highest external pushing force.23 To investigate the effect of external load resistance on the output performance of the transparent TENG device, the output current and averaged power density were described. Figure 6a shows the measured output current of the transparent TENG device with different external load resistances in the range of 0.5 to 100 MΩ. These measurements of the transparent TENG device with the different load resistances were performed under the external pushing force and frequency of 0.1-0.3 kgf and 1 Hz, respectively. During the measurements, the contacting area between the top electrode and dielectric (SWA PDMS) material was observed as 1 cm2, and the area of SWA PDMS of the TENG device during the measurement was also indicated in Figure S4 (See the Supporting Information). In Figure 6a, the output current was gradually decreased with increasing the load resistance due to Ohmic losses. The average output current (ISC) values were observed as ∼0.99, 0.82, 0.74, 0.61, 0.55, 0.33, 0.25, and 0.22 µA for the load resistance of 0.5, 1, 10, 30, 50, 70, 90 and 100 MΩ , respectively. To calculate the averaged power density, we assumed that the electric energy was equivalent to the Joule heating energy. Thus, the averaged power density was obtained by: 28,49 N

t2 i

i =1

t1i

∑R∫

I i2 (t ) dt N (t2 i − t1i )

,

where N is the number of peaks, R is the external load resistance and I (t) is the output current as a function of time. And the time between t1i and t2i is the interval time of ith peak of the measured current. Figure 6b shows the variation of obtained average power density per unit area of the transparent TENG device as a function of load resistance. It was found that the maximum average power density (Wavg) value of ∼0.75 mW/m2 was achieved at a load resistance of 50 MΩ. Finally, the robustness of the transparent TENG device was tested by measuring the output 13



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 14 of 30

voltage and current for 2000 sec (i.e., 1000 cycles), as shown in Figure 6c and 6d. These voltage and current measurements were performed under 0.3-0.5 kgf of external pushing force and 0.5 Hz of frequency. The transparent TENG device with SWA PDMS as a triboelectric material exhibited a consistently similar tendency in both the output voltage and current even after 1000 cycles without any significant degradation. Thus, these stable and continuous output voltage and current results up to 1000 cycles strongly support that the SWAs on PDMS were maintainable to produce triboelectric charges for many operating cycles.

CONCLUSIONS In summary, we demonstrated the highly-transperent and flexible TENG device with SWA PDMS layer as the triboelctric material, fabricated by a simple and cost-effective process. The PDMS layer with SWAs was prepared by the replication from the nanoporous AAO template as a mold. The SWA PDMS on ITO/PET exibited the relatively high tansmittance, which leads to the TENG device with transmittance of about 70% over a wavelength region of 400-1000 nm. The transparent TENG device with bare ITO/PET top electrode exhibited the higher output performance as compared to the TENG device with Au coated ITO/PET as the top electrode. Under 0.3 kgf external pushing force, the VOC and ISC values of the transparent TENG device (bare ITO/PET as the top electrode) were obtained to be ∼ 3.8 V and ∼ 0.8 µA, respectively, at an external pushing frequency of 0.5 Hz. Furthermore, the output performance of the transparent TENG device was observed at different external pushing frequencies and pushing forces, indicating the improved device performance due to the large friction and contact area between the two electrodes. The maximum Wavg value of ∼0.75 mW/m2 was achieved at a load resistance

14


Page 15 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


of 50 MΩ. These fabrication method and results can be useful to achieve transparent, flexible, and cost-effective TENG devices with high output performance.

Supporting Information The Supporting Information is available free of charge on the Internet at http://pubs.acs.org SEM image of the SWAs prepared by soft PDMS (Figure S1), PDMS spin-coating conditions, photographic images of pushing load cell and Indicator (Figure S2), TENG device performance with different spacer thickness (Figure S3), area of SWA PDMS layer laminated on the ITO/PET of TENG device (Figure S4).

Corresponding Author *Email: [email protected] (Prof. J. S. Yu)

Acknowledgements This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (No. 2014-069441).

References (1) Wang, Z. L.; Wu, W. Nanotechnology-Enabled Energy Harvesting for Self-Powered Micro/Nanosystems. Angew. Chem. Int. Ed. 2012, 51, 11700-11721. (2) Robel, I.; Subramanian, V.; Kuno, M.; Kamat, P. V. Quantum Dot Solar Cells. Harvesting Light Energy with CdSe Nanocrystals Molecularly Linked to Mesoscopic TiO2 Films. J. Am. Chem. Soc. 2006, 128, 2385-2393.

15



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 16 of 30

(3) Chang, C.; Tran, V. H.; Wang, J.; Fuh, Y. K.; Lin, L. Direct-Write Piezoelectric Polymeric Nanogenerator with High Energy Conversation Efficiency. Nano Lett. 2010, 10, 726-731. (4) Chen, X.; Xu, S.; Yao, N.; Shi, Y. 1.6 V Nanogenerator for Mechanical Energy Harvesting Using PZT Nanofibers. Nano Lett. 2010, 10, 2133-2137. (5) Ko, Y. H.; Lee, S. H.; Yu, J. S. Performance enhanced piezoelectric ZnO Nanogenerators With Highly Rough Au Electrode Surfaces on ZnO Submicrorod Arrays. Appl. Phys. Lett. 2013, 103, 022911. (6) Zhang, C.; Tang, W.; Han, C.; Fan, F.; Wang, Z. L. Theoretical Comparison, Equivalent Transformation, and Conjunction Operations of Electromagnetic Induction Generator and Triboelectric Nanogenerator for Harvesting Mechanical Energy. Adv. Mater. 2014, 26, 35803591. (7) Yang, Y.; Guo, W.; Pradel, K. C.; Zhu, G.; Zhou, Y.; Zhang, Y.; Hu, Y.; Lin, L.; Wang, Z. L. Pyroelectric Nanogenerators for Harvesting Thermoelectric Energy. Nano Lett. 2012, 12, 2833-2838. (8) Yang, W.; Chen, J.; Zhu, G.; Yang, J.; Bai, P.; Su, Y.; Jing, Q.; Cao, X.; Wang, Z. L. Harvesting Energy from the Natural Vibration of Human Walking. ACS Nano 2013, 7, 11317-11324. (9) Zhu, G.; Bai, P.; Chen, J.; Wang, Z. L. Power-generating Shoe Insole Based on Triboelectric Nanogenerators for Self-Powered Consumer Electronics. Nano Energy 2013, 2, 688-692. (10) Chen, J.; Yang, J.; Li, Z.; Fan, X.; Zi, Y.; Jing, Q.; Guo, H.; Wen, Z.; Pradel, K. C.; Niu, S.; Wang, Z. L. Networks of Triboelectric Nanogenerators for Harvesting Water Wave Energy: A Potential Approach toward Blue Energy. ACS Nano 2015, 9, 3324-3331.

16


Page 17 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


(11) Chen, J.; Zhu, G.; Yang, W.; Jing, Q.; Bai, P.; Yang, Y.; Hou, T. C.; Wang, Z. L. HarmonicResonator-Based Triboelectric Nanogenerator as a Sustainable Power Source and a SelfPowered Active Vibration Sensor. Adv. Mater. 2013, 25, 6094-6099. (12) Yang, W.; Chen, J.; Jing, Q.; Yang, J.; Wen, X.; Su, Y.; Zhu, G.; Bai, P.; Wang, Z. L. 3D Stack Integrated Triboelectric Nanogenerator for Harvesting Vibration Energy. Adv. Funct. Mater. 2014, 24, 4090-4096. (13) Guo, H.; Chen, J.; Yeh, M. H.; Fan, X.; Wen, Z.; Li, Z.; Hu, C.; Wang, Z. L. An Ultrarobust High-Performance Triboelectric Nanogenerator Based on Charge Replenishment. ACS Nano 2015, 9, 5577-5584. (14) Zhu, G.; Chen, J.; Zhang, T.; Jing, Q.; Wang, Z. L. Radial-Arrayed Rotary Electrification for High Performance Triboelectric Generator. Nat. Commun. 2014, 5, 3426. (15) Wang, Z. L. Triboelectric Nanogenerators as New Energy Technology for Self-Powered Systems and as Active Mechanical and Chemical Sensors. ACS Nano 2013, 7, 9533-9557. (16) Yang, W.; Chen, J.; Wen, X.; Jing, Q.; Yang, J.; Su, Y.; Zhu, G.; Wu, W.; Wang, Z. L. Triboelectrification Based Motion Sensor for Human-Machine Interfacing. ACS Appl. Mater. Interfaces 2014, 6, 7479-7484. (17) Yang, J.; Chen, J.; Su, Y.; Jing, Q.; Li, Z.; Yi, F.; Wen, X.; Wang, Z.; Wang, Z. L. EardrumInspired Active Sensors for Self-Powered Cardiovascular System Characterization and Throat-Attached Anti-Interference Voice Recognition. Adv. Mater. 2015, 27, 1316-1326. (18) Chen, J.; Zhu, G.; Yang, J.; Jing, Q.; Bai, P.; Yang, W.; Qi, X.; Su, Y.; Wang, Z. L. Personalized Keystroke Dynamics for Self-Powered Human-Machine Interfacing. ACS Nano 2015, 9, 105-116.

17



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 18 of 30

(19) Bai, P.; Zhu, G.; Jing, Q.; Wu, Y.; Yang, J.; Chen, J.; Ma, J.; Zhang, G.; Wang, Z. L. Transparent and Flexible Barcode Based on Sliding Electrification for Self-Powered Identification Systems. Nano Energy 2015, 12, 278-286. (20) Zhu, G.; Yang, W. Q.; Zhang, T.; Jing, Q.; Chen, J.; Zhou, Y. S.; Bai, P.; Wang, Z. L. SelfPowered, Ultrasensitive, Flexible Tactile Sensors Based on Contact Electrification. Nano Lett. 2014, 14, 3208-3213. (21) Lin, L.; Hu, Y.; Xu, C.; Zhang, Y.; Zhang, R.; Wen, X.; Wang, Z. L. Transparent Flexible Nanogenerator as Self-Powered Sensor for Transportation Monitoring. Nano Energy 2013, 2, 75-81. (22) Choi, M. Y.; Choi, D.; Jin, M. J.; Kim, I.; Kim, S. H.; Choi, J. Y.; Lee, S. Y.; Kim, J. M.; Kim, S. W. Mechanically Powered Transparent Flexible Charge-Generating Nanodevices with Piezoelectric ZnO Nanorods. Adv. Mater. 2009, 21, 2185-2189. (23) Ko, Y. H.; Nagaraju, G.; Lee, S. H.; Yu, J. S. PDMS-based Triboelectric and Transparent Nanogenerators with ZnO Nanorod Arrays. ACS Appl. Mater. Inter. 2014, 6, 6631-6637. (24) Wang, Z. L. Triboelectric Nanogenerators as New Energy Technology and Self-Powered Sensors–Principles, Problems and Perspectives. Faraday Discuss. 2014, 176, 447. (25) Wang, Z. L.; Chen, J.; Lin, L. Progress in Triboelectric Nanogenerators as a New Energy Technology and Self-Powered Sensors. Energy Environ. Sci. 2015, 8, 2250-2282. (26) Zhu, G.; Peng, B.; Chen, J.; Jing, Q.; Wang, Z. L. Triboelectric Nanogenerators as a New Energy Technology: From Fundamentals, Devices, to Applications. Nano Energy 2015, 14, 126-138. (27) Ko, Y. H.; Lee, S. H.; Leem, J. W.; Yu, J. S. High Transparency and Triboelectric Charge Generation Properties of Nano-patterned PDMS. RSC Adv. 2014, 4, 10216-10220.

18


Page 19 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


(28) Zhu, G.; Lin, Z. H.; Jing, Q.; Bai, P.; Pan, C.; Yang, Y.; Zhou, Y.; Wang, Z. L. Toward LargeScale Energy Harvesting by a Nanoparticle-Enhanced Triboelectric Nanogenerator. Nano Lett. 2013, 13, 847-853. (29) Fan, F. R.; Lin, L.; Zhu, G.; Wu, W.; Zhang, R.; Wang, Z. L. Transparent Triboelectric Nanogenerators and Self-Powered Pressure Sensors Based on Micropatterned Plastic Films. Nano Lett. 2012, 12, 3109-3114. (30) Fan, FR.; Tian, Z. Q.; Wang, Z. L. Flexible Triboelectric Generator. Nano energy 2012, 1, 328-334. (31) Boden, S.A.; Bagnall, D.M. Tunable Reflection Minima of Nanostructured Antireflective Surfaces. Appl. Phys. Lett. 2008, 93, 133108. (32) Yu, Z.; Gao, H.; Wu, W.; Ge, H.; Chou, S. Y. Fabrication of Large Area Subwavelength Antireflection Structures on Si Using Trilayer Resist Nanoimprint Lithography and Liftoff. J. Vac. Sci. Technol. B 2003, 21, 2874-2877. (33) Song, Y. M.; Choi, H. J.; Yu, J. S.; Lee, Y. T. Design of Highly Transparent Glasses With Broadband Antireflective Subwavelength Structures. Opt. Express 2010, 18, 13063-13071. (34) Leem, J. W.; Song, Y. M.; Yu, J. S. Six-fold Hexagonal Symmetric Nanostructures With Various Periodic Shapes on GaAs Substrates for Efficient Antireflection and Hydrophobic Properties. Nanotechnology 2011, 22, 485304. (35) Lee, W.; Park, S. J. Porous Anodic Aluminum Oxide: Anodization and Templated Synthesis of Functional Nanostructures. Chem. Rev. 2014, 114, 7487-7556. (36) Kokonou, M.; Nassiopoulou, A. G.; Giannakopoulos, K. P. Ultra-Thin Porous Anodic Alumina Films with Self-Ordered Cylindrical Vertical Pores on a p-Type Silicon Substrate. Nanotechnology 2005, 16, 103-106.

19



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 20 of 30

(37) Schmid, H.; Michel, B. Siloxane Polymers for High-Resolution, High-Accuracy Soft Lithography. Macromolecules 2000, 33, 3042-3049. (38) Truong, T. T.; Lin, R.; Jeon, S.; Lee, H. H.; Maria, J.; Gaur, A.; Hua, F.; Meinel, I.; Rogers, J. A. Soft Lithography Using Acryloxy Perfluoropolyether Composite Stamps. Langmuir 2007, 23, 2898-2905. (39) Odom, T. W.; Love, J. C.; Wolfe, D. B.; Paul, K. E.; Whitesides, G. M. Improved Pattern Transfer in Soft Lithography Using Composite Stamps. Langmuir 2002, 18, 5314-5320. (40) Choi, K. M.; Rogers, J. A. A Photocurable Poly(dimethylsiloxane) Chemistry Designed for Soft Lithographic Molding and Printing in the Nanometer Regime. J. Am. Chem. Soc. 2003, 125, 4060-4061. (41) Leem, J. W.; Kim, S.; Lee, S. H.; Rogers, J. A.; Kim, E.; Yu, J. S. Efficiency Enhancement of Organic Solar Cells Using Hydrophobic Antireflective Inverted Moth-Eye Nanopatterned PDMS Films. Adv. Energy Mater. 2014, 4, 1301315. (42) Fan, F. R.; Luo, J.; Tang, W.; Li, C.; Zhang, C.; Tian, Z.; Wang, Z. L. Highly Transparent and Flexible Triboelectric Nanogenerators: Performance Improvements and Fundamental Mechanisms. J. Mater. Chem. A 2014, 2, 13219-13225. (43) Lim, J. H.; Ko, Y. H.; Leem, J. W.; Yu, J. S. Improvement in Light Harvesting of DyeSensitized Solar Cells With Antireflective and Hydrophobic Textile PDMS Coating by Facile Soft Imprint Lithography. Opt. Express 2015, 23, A169-A179. (44) Cross, J. A. Electrostatics: Principles, Problems and Applications; Adam Hilger: Bristol, U.K., 1987.

20


Page 21 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


(45) Zhang, X. S.; Han, M. D.; Wang, R. X.; Meng, B.; Zhu, F. Y.; Sun, X. M.; Hu, W.; Wang, W. Li, Z. H.; Zhang H. X. High-Performance Triboelectric Nanogenerator with Enhanced Energy Density Based on Single-Step Fluorocarbon Plasma Treatment. Nano Energy 2014, 4, 123-131. (46) Wang, S.; Lin, L.; Wang, Z. L. Nanoscale Triboelectric-Effect-Enabled Energy Conversion for Sustainably Powering Portable Electronics. Nano Lett. 2012, 12, 6339-6346. (47) Han, M.; Zhang, X. S.; Meng, B.; Liu, W.; Tang, W.; Sun, X.; Wang, W.; Zhang, H. r‑Shaped Hybrid Nanogenerator with Enhanced Piezoelectricity. ACS Nano 2013, 7, 8554-8560. (48) Tian, H.; Ma, S.; Zhao, H. M.; Wu, C.; Ge, J.; Xie, D.; Yang, Y.; Ren, T. L. Flexible Electrostatic nanogenerator using Graphene Oxide Film. Nanoscale 2013, 5, 8951-8957. (49) Niu, S.; Wang, S.; Lin, L.; Liu, Y.; Zhou, Y. S.; Hua, Y.; Wang, Z. L. Theoretical Study of Contact-Mode Triboelectric Nanogenerators as An Effective Power Source. Energy Environ. Sci. 2013, 6, 3576-3583. (50) Tang, W.; Zhou, T.; Zhang, C.; Fan, F. R.; Han, C. B.; Wang, Z. L. A Power-Transformedand-Managed Triboelectric Nanogenerator and Its Applications in a Self-Powered Wireless Sensing Node. Nanotechnology 2014, 25, 225402. (51) Zhang, X. S.; Han, M. D.; Wang, R.X.; Zhu, F. Y.; Li, Z. H.; Wang, W.; Zhang, H. X. Frequency-Multiplication

High-Output

Triboelectric

Nanogenerator

for

Sustainably

Powering Biomedical Microsystems. Nano Lett. 2013, 13, 1168-1172. (52) Zhu, G.; Pan, C.; Guo, W.; Chen, C. Y.; Zhou, Y.; Yu, R.; Wang, Z. L. TriboelectricGenerator-Driven Pulse Electrodeposition for Micropatterning. Nano Lett. 2012, 12, 49604965.

21



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 22 of 30

Figure captions Figure 1. Schematic for the fabrication of the TENG device with the SWA PDMS layer laminated on the ITO/PET substrate as a bottom electrode and the bare ITO/PET as a top electrode. The schematics of two different TENG devices (Device I and II) are also shown. Figure 2. (a) Contour plot of variation of the calculated transmittance spectra of SWA PDMS on ITO/PET as functions of wavelength and diameter to period ratio, and RDP of SWAs. (b) Measured transmittance spectra of the TENG devices and their constituent materials in the range of wavelengths from 380 to 1000 nm. Figure 3. (a) Top-view and cross-sectional SEM images of the nanoporous AAO template on Si substrate (i & iii) and the SWA PDMS (ii & iv) replicated by the AAO template. Inset of (a) (iv) also shows the total thickness of the replicated PDMS layer. (b) Photographs of the flat and SWA PDMS layers on ITO/PET and the water droplets on the corresponding samples. Figure 4. (a) Schematic illustration of the charge distribution process at each step of the TENG device and its working principle. Measured (b) VOC and (c) ISC curves of the TENG devices using (i) ITO/PET and (ii) Au coated ITO/PET as a top electrodes, during the measurements pushing frequency and pushing force are maintained at 0.5 Hz and 0.3 kgf, respectively. For comparison, the measured VOC and ISC curves of the TENG device fabricated by the flat PDMS on ITO/PET were compared in figure (d). Figure 5. (a) Photographic images of the fabricated transparent TENG device for (i) high transparency, (ii) good flexibility, and (iii) pushing test with the TENG device. Measured (i) VOC and (ii) ISC curves: (b) under different external pushing frequencies from 1 to 4 Hz at 0.3 kgf of external pushing force and (c) under 1 Hz of external pushing frequency at different external pushing forces. Figure 6. (a) Measured output current of the transparent TENG device at different load resistances under external pushing force in the range of 0.1-0.3 kgf and external pushing frequency of 1 Hz. (b) Obtained average power density values of the transparent TENG device 22


Page 23 of 30

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


as a function of load resistance. Robustness test of the transparent TENG: (c) Output voltage and (d) current of the TENG device for 2000 sec (i.e., 1000 cycles) under 0.3-0.5 kgf of external pushing force and 0.5 Hz of frequency.

23



Figure. 1 Anodization Al Si

AAO Si

Al deposited on Si substrate

Anodic Aluminum Oxide (AAO) on Si substrate

Device-I

PDMS AAO

Si

Pouring PDMS solution

Curing

Peeling off

Spacer

Spacer

ITO/PET

SWA PDMS layer ITO/PET

Device-II

SWA PDMS layer

SWA PDMS

ITO/PET

SWA PDMS layer

SWA PDMS layer

Spacer

Au/ITO/PET

Spacer

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 24 of 30

Laminated PDMS on ITO/PET

ITO/PET

Triboelectric nano generators

24


Page 25 of 30

(a)

Diameter to Period Ratio of SWA PDMS

Figure. 2

1.0

SWA PDMS (100 µm)

0.9

PET (130 µm) ITO (200 nm)

85 %

0.8 0.7

85 %

0.6

Transmittance (%) >9595 90

0.5

70

0.4

(b)

75 60

0.3 300

50 400

500

600

700

45

800

30 30

Wavelength (nm) 90 SWA PDMS on ITO/PET

85

Total Transmittance (%)

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


80 ITO/PET

75

Flat PDMS on ITO/PET

Device-I

70 65 60 2 1 0

Au/ITO/PET Device-II

400

500

600

700

800

900

1000

Wavelength (nm)

25



1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 26 of 30

Figure. 3

(a)

(ii)

(i)

100 nm

100 nm

(iv)

(iii)

∼100 µm

100 nm

(b)

100 nm

Flat PDMS on ITO/PET

SWA PDMS on ITO/PET

30 µm

θCA~ 93o

θCA~ 115o

Flat PDMS

SWA PDMS

26


Page 27 of 30

Figure. 4 (a) A

I. Initial state

Force Force +

+

+

e-

+

+++ ++

A

+- +- + - +- +- + + - - +- +- +++ - - - +-+- + - +- +- +-

++++ +

A

V. Pressing II. Pressed Force ----- ++ +++ +

-- - - - -----

+ +++

+ +++

(b)

+ + ++

3

2

2

1 0 -1 -2 -3

1 0 -1 -2 -3

External pushing force: 0.1-0.3 kgf External pushing frequency: 0.5 Hz

-4 0

2

4

6

8

10

12

14

16

18


-4 -5

20

0

2

4

6

Time (Sec)

(c) 1.2

(i)

8

10

12

14

16

18

20

Time (sec) 1.2

Device - Ι

Pressing

0.8

0.8

0.4

0.4

Current (µA)

Current (µA)

Device - ΙΙ

(ii)

4

Voltage (V)

Voltage (V)

5

Device - Ι

(i)

3

-5

A

III. Releasing

5 4

e-

+ -- ++++++ + +++ ---- - - -- - -- + + + + + + +

A

IV. Released

0.0 -0.4

Device - ΙΙ

(ii) Pressing

0.0 -0.4

Releasing -0.8

-0.8

Releasing -1.2 0

2

4

External pushing force: 0.1-0.3 kgf External pushing frequency: 0.5 Hz 6

8

10

12

14

16

18

-1.2 0

20

External pushing force: 0.1-0.3 kgf External pushing frequency: 0.5 Hz 2

4

6

Time (sec)

(d)

5 4

Triboelectric material: Flat PDMS

8

10

12

14

16

18

20

Time (sec) 0.4

Device - Ι

Device - Ι

Triboelectric material: Flat PDMS

3 0.2

Current (µA)

2

Voltage (V)

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


1 0 -1 -2

-0.2

-3 External pushing force: 0.1-0.3 kgf External pushing frequency: 0.5 Hz

-4 -5 0

0.0

4

8

12

Time (sec)

16


20

-0.4 0

2

4

6

8

10

12

14

16

18

20

Time (sec)

27



Figure. 5

(a)

(ii)

(i)

(iii)

1 cm

Releasing

1 cm

(i) Pushing force: 0.1-0.3 kgf

2.0

10

1.0

Current (µA)

Voltage (V)

(ii) Pushing force: 0.1-0.3 kgf

1.5

5 0 -5

1 Hz

2 Hz

-10

0

20

40

0.5 0.0 -0.5 -1.0

1 Hz

-1.5

3 Hz

-2.0

4 Hz

Various pushing frequency: -15

Pressing

2.5

15

(b)

60

80

-2.5

100

2 Hz 3 Hz

Various pushing frequency: 0

20

40

Time (sec)

4 Hz

60

80

100

Time (sec)

15

(c)

2.0

(i) Pushing frequency: 1 Hz

(ii) Pushing frequency: 1 Hz

1.5

10

1.0 5

Current (µA)

Voltage (V)

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 28 of 30

0 -5

0.5 0.0 -0.5 -1.0

0.3-0.5 Kgf

0.9-1.1 Kgf

1.7-1.9 Kgf

-1.5

0.3-0.5 Kgf

-10 -2.0

Various pushing force: 0

20

40

60

80

0.9-1.1 Kgf

Various pushing force: 0

10

20

30

40

1.7-1.9 Kgf 50 60 70

80

Time (sec)

Time (sec)

28


Page 29 of 30

Figure. 6 (b) 1.2

Current (µA)

0.8 0.4 0.0 -0.4

70 MΩ Ω

0.5 MΩ Ω

0

20

90 MΩ Ω 100 MΩ Ω

Ω 30 MΩ Ω 50 MΩ

10 MΩ Ω

-0.8 -1.2

0.7

40

0.6 0.5 0.4 0.3 0.2 0.1

1 MΩ Ω

60

80

100

120

140

0.0

160

0

10

20

30

40

50

60

70

80

90

100

Load Resistance (MΩ)

Time (Sec)

(c)

0.8

2

External pushing force: 0.1-0.3 kgf External pushing frequency: 1 Hz

Power Density (mW/m )

(a)

(d)

8

1.5 External pushing frequency: 0.5 Hz

External pushing frequency: 0.5 Hz

6 1.0

4 2

Current (µA)

Voltage (V)

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


0 -2

0.5 0.0 -0.5

-4 -1.0

-6 -8

External pushing force: 0.3-0.5 kgf

1

10

100

1000

-1.5

External pushing force: 0.3-0.5 kgf

1

Time (sec)

10

100

1000

Time (sec)

29



Table of Contents (TOC) Graphic SWA PDMS Layer

Self-cleaning

3

Pushing force: 0.1-0.3 kgf

2

100 nm

Transparent TENG

SWA PDMS Flexible TENG

Current (µA)

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 30 of 30

1 0 -1 -2 -3

1 Hz

2 Hz 3 Hz

Various pushing frequency:

0

20

40

60

4 Hz 80

100

Time (sec)

30


Highly Transparent and Flexible Triboelectric Nanogenerators with

Recommend Documents